Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add filters








Language
Year range
1.
Journal of the Korean Pediatric Society ; : 879-882, 1999.
Article in Korean | WPRIM | ID: wpr-186769

ABSTRACT

Transient neonatal pustular melanosis(TNPM) is a benign, self-limited, cutaneous disorder of unknown etiology. Significant physical findings are limited to the skin. Hematologic and serological tests are normal. Cultures of blood and pustule are negative. Biopsy specimens from pustules show a intracorneal or subcorneal separation containing neutrophils and also some eosinophils. TNPM produces only cutaneous lesions and requires no treatment. So it is essential to differentiate TNPM and other neonatal skin lesions. We experienced a case of TNPM in a male newborn with generalized superficial vesicopustules which developed into pigmented macules and report this case with review of related literatures.


Subject(s)
Humans , Infant, Newborn , Male , Biopsy , Eosinophils , Melanosis , Neutrophils , Serologic Tests , Skin
2.
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 256-261, 1999.
Article in Korean | WPRIM | ID: wpr-8043

ABSTRACT

Ileus caused by impaction of hardened residual barium stagnated in the colon, a rare complication of barium-enema examination, constitutes a particularly serious problem when it occurs in congenital megacolon patients. The administration of gastrografin in such case has proven efficacy in dissolution of impacted barium refratory to routine means of evacuation. We experienced a case of barium-impaction occurred in 6-months old male who had congenital megacolon. Gastrografin enema was a safe and simple method used in the management of this case.


Subject(s)
Humans , Infant , Male , Barium , Colon , Diatrizoate Meglumine , Enema , Hirschsprung Disease , Ileus
3.
Korean Journal of Pediatric Hematology-Oncology ; : 155-160, 1997.
Article in Korean | WPRIM | ID: wpr-7101

ABSTRACT

The leukemia of infancy, characterized by a high leukocyte count, massive organomegaly, CNS leukemia at diagnosis, high chromosomal abnormalities and immature phenotype. This is reflected in its poor prognosis. Isolated lesions of the facial nerve have been reported in leukemia patients, but appear to be rare in infancy. We report a case of unilateral facial nerve paralysis occurred in 4-months-old male who had acute lymphoblastic leukemia with review of literature.


Subject(s)
Humans , Infant , Male , Chromosome Aberrations , Diagnosis , Facial Nerve , Leukemia , Leukocyte Count , Paralysis , Phenotype , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Prognosis
SELECTION OF CITATIONS
SEARCH DETAIL